Rapid Review·Cardiovascular

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Cardiomyopathy

T1Must know

Cardiomyopathy

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Key takeaways

a cardiomyopathy is a disease of the heart muscle itself, acquired or inherited.
  • It impairs the pump, leading to arrhythmias and heart failure.
  • Ischemic workup: rule out coronary disease first.
  • Transthoracic echocardiography (TTE): sorts the type by chamber size, wall thickness and systolic function.
Dilated Cardiomyopathy, Hypertrophic Cardiomyopathy, Restrictive Cardiomyopathy, Takotsubo Cardiomyopathy, Peripartum Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy.
the heart failure drugs (Heart Failure).
  • Beta blocker.
  • Angiotensin-converting enzyme (ACE) inhibitor, angiotensin receptor blocker (ARB) or angiotensin receptor-neprilysin inhibitor (ARNI, sacubitril/valsartan).
  • Mineralocorticoid receptor antagonist.
  • Sodium-glucose cotransporter-2 (SGLT2) inhibitor.
for symptoms, particularly volume overload; first line in DCM.
chosen by the cause of the cardiomyopathy.

How it's tested

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High-yield images2
Working up a cardiomyopathy: an ischemic workup, then a transthoracic echo sorts it. Dilated: larger chambers with thin walls and reduced systolic function. Hypertrophic: thick left ventricular walls, normal or small cavity, usually preserved systolic function. Restrictive: diastolic dysfunction with normal or mildly thick walls and normal or slightly reduced systolic function. Stress-induced: akinesis of the apex. All get treatment of the underlying disease and guideline-directed therapy.
The three structural cardiomyopathies beside a normal heart. Hypertrophic: a thicker left ventricular wall with septal predominance. Dilated: ventricular dilation with thin walls and possible atrial dilation. Restrictive: stiff ventricles with dilated atria.

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